Pharmaceutically active diketopiperazines

PCT No. PCT/GB93/01734 Sec. 371 Date Apr. 11, 1995 Sec. 102(e) Date Apr. 11, 1995 PCT Filed Aug. 16, 1993 PCT Pub. No. WO94/04512 PCT Pub. Date Mar. 3, 1994Diketopiperazines of the formula: ame or different, is independently selected from the group consisting of hydrogen, C1-C6 alkyl unsubstituted o...

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Hauptverfasser: JUSTIN STEPHEN BRYANS, MARK ANTHONY DAVID COLLINS, MARIA INOES CHICARELLI-ROBINSON, STEPHEN JAMES BROCCHINI, CHRISTOPHER JOHN LATHAM, JOHN RICHARDSON SHAW
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creator JUSTIN STEPHEN BRYANS
MARK ANTHONY DAVID COLLINS
MARIA INOES CHICARELLI-ROBINSON
STEPHEN JAMES BROCCHINI
CHRISTOPHER JOHN LATHAM
JOHN RICHARDSON SHAW
description PCT No. PCT/GB93/01734 Sec. 371 Date Apr. 11, 1995 Sec. 102(e) Date Apr. 11, 1995 PCT Filed Aug. 16, 1993 PCT Pub. No. WO94/04512 PCT Pub. Date Mar. 3, 1994Diketopiperazines of the formula: ame or different, is independently selected from the group consisting of hydrogen, C1-C6 alkyl unsubstituted or substituted by one or more halogen atoms, C1-C6 alkoxy, C1-C6 alkylthio, halogen, hydroxy, nitro, phenyl, -cyano, -CH2OH, -CH2COOH, -CO2R11, -NHCOR11, -NHSO2R13, -SO2R13, -CON(R11R12), -SOR13, -SO2N(R11R12), -N(R11R12), and -O(CH2)nN(R11R12), -O(CH2)nCO2R11, -OCOR11, -CH2OCOR11, -CH2NHCOR11, -CH2NHCOOR13, -CH2SR11, -CH2SCOR11, -CH2S(O)mR13 wherein m is 1 or 2, -CH2NHCO(CH2)nCO2R11, -N(R11)COR12, -NHCOCF3, -NHCO(CH2)nCO2R11, -NHCO(CH2)nOCOR11 and -NHCO(CH2)nOR11 wherein n is 0 or is an integer of from 1 to 6, each of R11 and R12 is independently H or C1-C6 alkyl and R13 is C1-C6 alkyl; or any of R1 and R2, R2 and R3, R3 and R4 and R4 and R5, or R6 and R7, R7 and R8, R8 and R9 and R9 and R10, form together with the carbon atoms to which they are attached a benzene ring; and pharmaceutically acceptable salts and esters thereof are inhibitors of the plasminogen activator inhibitor.
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fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_GB2284420B</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>GB2284420B</sourcerecordid><originalsourceid>FETCH-epo_espacenet_GB2284420B3</originalsourceid><addsrcrecordid>eNrjZNAMyEgsyk1MTi0tyUxOzMmpVEhMLsksS1VIycxOLckvyCxILUqsysxLLeZhYE1LzClO5YXS3Azybq4hzh66qQX58anFBUAz8lJL4t2djIwsTEyMDJyMCasAALZjKJg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Pharmaceutically active diketopiperazines</title><source>esp@cenet</source><creator>JUSTIN STEPHEN BRYANS ; MARK ANTHONY DAVID COLLINS ; MARIA INOES CHICARELLI-ROBINSON ; STEPHEN JAMES BROCCHINI ; CHRISTOPHER JOHN LATHAM ; JOHN RICHARDSON SHAW</creator><creatorcontrib>JUSTIN STEPHEN BRYANS ; MARK ANTHONY DAVID COLLINS ; MARIA INOES CHICARELLI-ROBINSON ; STEPHEN JAMES BROCCHINI ; CHRISTOPHER JOHN LATHAM ; JOHN RICHARDSON SHAW</creatorcontrib><description>PCT No. PCT/GB93/01734 Sec. 371 Date Apr. 11, 1995 Sec. 102(e) Date Apr. 11, 1995 PCT Filed Aug. 16, 1993 PCT Pub. No. WO94/04512 PCT Pub. Date Mar. 3, 1994Diketopiperazines of the formula: ame or different, is independently selected from the group consisting of hydrogen, C1-C6 alkyl unsubstituted or substituted by one or more halogen atoms, C1-C6 alkoxy, C1-C6 alkylthio, halogen, hydroxy, nitro, phenyl, -cyano, -CH2OH, -CH2COOH, -CO2R11, -NHCOR11, -NHSO2R13, -SO2R13, -CON(R11R12), -SOR13, -SO2N(R11R12), -N(R11R12), and -O(CH2)nN(R11R12), -O(CH2)nCO2R11, -OCOR11, -CH2OCOR11, -CH2NHCOR11, -CH2NHCOOR13, -CH2SR11, -CH2SCOR11, -CH2S(O)mR13 wherein m is 1 or 2, -CH2NHCO(CH2)nCO2R11, -N(R11)COR12, -NHCOCF3, -NHCO(CH2)nCO2R11, -NHCO(CH2)nOCOR11 and -NHCO(CH2)nOR11 wherein n is 0 or is an integer of from 1 to 6, each of R11 and R12 is independently H or C1-C6 alkyl and R13 is C1-C6 alkyl; or any of R1 and R2, R2 and R3, R3 and R4 and R4 and R5, or R6 and R7, R7 and R8, R8 and R9 and R9 and R10, form together with the carbon atoms to which they are attached a benzene ring; and pharmaceutically acceptable salts and esters thereof are inhibitors of the plasminogen activator inhibitor.</description><edition>6</edition><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>1996</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19960925&amp;DB=EPODOC&amp;CC=GB&amp;NR=2284420B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19960925&amp;DB=EPODOC&amp;CC=GB&amp;NR=2284420B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JUSTIN STEPHEN BRYANS</creatorcontrib><creatorcontrib>MARK ANTHONY DAVID COLLINS</creatorcontrib><creatorcontrib>MARIA INOES CHICARELLI-ROBINSON</creatorcontrib><creatorcontrib>STEPHEN JAMES BROCCHINI</creatorcontrib><creatorcontrib>CHRISTOPHER JOHN LATHAM</creatorcontrib><creatorcontrib>JOHN RICHARDSON SHAW</creatorcontrib><title>Pharmaceutically active diketopiperazines</title><description>PCT No. PCT/GB93/01734 Sec. 371 Date Apr. 11, 1995 Sec. 102(e) Date Apr. 11, 1995 PCT Filed Aug. 16, 1993 PCT Pub. No. WO94/04512 PCT Pub. Date Mar. 3, 1994Diketopiperazines of the formula: ame or different, is independently selected from the group consisting of hydrogen, C1-C6 alkyl unsubstituted or substituted by one or more halogen atoms, C1-C6 alkoxy, C1-C6 alkylthio, halogen, hydroxy, nitro, phenyl, -cyano, -CH2OH, -CH2COOH, -CO2R11, -NHCOR11, -NHSO2R13, -SO2R13, -CON(R11R12), -SOR13, -SO2N(R11R12), -N(R11R12), and -O(CH2)nN(R11R12), -O(CH2)nCO2R11, -OCOR11, -CH2OCOR11, -CH2NHCOR11, -CH2NHCOOR13, -CH2SR11, -CH2SCOR11, -CH2S(O)mR13 wherein m is 1 or 2, -CH2NHCO(CH2)nCO2R11, -N(R11)COR12, -NHCOCF3, -NHCO(CH2)nCO2R11, -NHCO(CH2)nOCOR11 and -NHCO(CH2)nOR11 wherein n is 0 or is an integer of from 1 to 6, each of R11 and R12 is independently H or C1-C6 alkyl and R13 is C1-C6 alkyl; or any of R1 and R2, R2 and R3, R3 and R4 and R4 and R5, or R6 and R7, R7 and R8, R8 and R9 and R9 and R10, form together with the carbon atoms to which they are attached a benzene ring; and pharmaceutically acceptable salts and esters thereof are inhibitors of the plasminogen activator inhibitor.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1996</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNAMyEgsyk1MTi0tyUxOzMmpVEhMLsksS1VIycxOLckvyCxILUqsysxLLeZhYE1LzClO5YXS3Azybq4hzh66qQX58anFBUAz8lJL4t2djIwsTEyMDJyMCasAALZjKJg</recordid><startdate>19960925</startdate><enddate>19960925</enddate><creator>JUSTIN STEPHEN BRYANS</creator><creator>MARK ANTHONY DAVID COLLINS</creator><creator>MARIA INOES CHICARELLI-ROBINSON</creator><creator>STEPHEN JAMES BROCCHINI</creator><creator>CHRISTOPHER JOHN LATHAM</creator><creator>JOHN RICHARDSON SHAW</creator><scope>EVB</scope></search><sort><creationdate>19960925</creationdate><title>Pharmaceutically active diketopiperazines</title><author>JUSTIN STEPHEN BRYANS ; MARK ANTHONY DAVID COLLINS ; MARIA INOES CHICARELLI-ROBINSON ; STEPHEN JAMES BROCCHINI ; CHRISTOPHER JOHN LATHAM ; JOHN RICHARDSON SHAW</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_GB2284420B3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1996</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><toplevel>online_resources</toplevel><creatorcontrib>JUSTIN STEPHEN BRYANS</creatorcontrib><creatorcontrib>MARK ANTHONY DAVID COLLINS</creatorcontrib><creatorcontrib>MARIA INOES CHICARELLI-ROBINSON</creatorcontrib><creatorcontrib>STEPHEN JAMES BROCCHINI</creatorcontrib><creatorcontrib>CHRISTOPHER JOHN LATHAM</creatorcontrib><creatorcontrib>JOHN RICHARDSON SHAW</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>JUSTIN STEPHEN BRYANS</au><au>MARK ANTHONY DAVID COLLINS</au><au>MARIA INOES CHICARELLI-ROBINSON</au><au>STEPHEN JAMES BROCCHINI</au><au>CHRISTOPHER JOHN LATHAM</au><au>JOHN RICHARDSON SHAW</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Pharmaceutically active diketopiperazines</title><date>1996-09-25</date><risdate>1996</risdate><abstract>PCT No. PCT/GB93/01734 Sec. 371 Date Apr. 11, 1995 Sec. 102(e) Date Apr. 11, 1995 PCT Filed Aug. 16, 1993 PCT Pub. No. WO94/04512 PCT Pub. Date Mar. 3, 1994Diketopiperazines of the formula: ame or different, is independently selected from the group consisting of hydrogen, C1-C6 alkyl unsubstituted or substituted by one or more halogen atoms, C1-C6 alkoxy, C1-C6 alkylthio, halogen, hydroxy, nitro, phenyl, -cyano, -CH2OH, -CH2COOH, -CO2R11, -NHCOR11, -NHSO2R13, -SO2R13, -CON(R11R12), -SOR13, -SO2N(R11R12), -N(R11R12), and -O(CH2)nN(R11R12), -O(CH2)nCO2R11, -OCOR11, -CH2OCOR11, -CH2NHCOR11, -CH2NHCOOR13, -CH2SR11, -CH2SCOR11, -CH2S(O)mR13 wherein m is 1 or 2, -CH2NHCO(CH2)nCO2R11, -N(R11)COR12, -NHCOCF3, -NHCO(CH2)nCO2R11, -NHCO(CH2)nOCOR11 and -NHCO(CH2)nOR11 wherein n is 0 or is an integer of from 1 to 6, each of R11 and R12 is independently H or C1-C6 alkyl and R13 is C1-C6 alkyl; or any of R1 and R2, R2 and R3, R3 and R4 and R4 and R5, or R6 and R7, R7 and R8, R8 and R9 and R9 and R10, form together with the carbon atoms to which they are attached a benzene ring; and pharmaceutically acceptable salts and esters thereof are inhibitors of the plasminogen activator inhibitor.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
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subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title Pharmaceutically active diketopiperazines
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